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Synthesis 1996; 1996(3): 361-366
DOI: 10.1055/s-1996-4222
DOI: 10.1055/s-1996-4222
paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved.
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or duplication of any kind, translating, preparation of microfilms, and electronic
data processing and storage.Synthetic Potentialities of Alkyl and Aryl Cyclopropylidenealkyl Sulfides: Access to 1-(Arylthio)vinylcyclopropanes by a 1,3-Shift of an Arylthio Group
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Publikationsverlauf
Publikationsdatum:
31. Dezember 2000 (online)

Alkyl and aryl cyclopropylidenealkyl sulfides 2, 4 and 5 were converted to give access to 1-(arylthio)vinylcyclopropanes 3 by light induced or acid catalyzed 1,3-shift of the arylthio group. Some results on the reactivity of sulfides 2, 4 and 5 are reported.
thia-allylic rearrangement - vinylcyclopropanes - cyclopropylidenealkylthioethers - sulphonium salts - Pd(0) catalyzed allylic nucleophilic substitutions